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Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

Fibroblast changes in systemic sclerosis may help understand disease severity and treatment.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Vemurafenib therapy can cause hair loss, but clobetasol propionate foam can help regrow hair.

Giant axonal neuropathy changes the structure of keratin in human hair.

A young woman had a rare scalp tumor usually found in older women.

The conclusion is that surgical removal of solitary fibrofolliculoma is effective with no relapses, and diagnosis requires a biopsy due to varied symptoms.

Multiple perifollicular fibromas may actually be unrecognized cases of Birt-Hogg-Dubé syndrome.

Giant axonal neuropathy changes the structure of keratin in human hair, making it stiffer and stronger.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

Type II spiral ganglion neurites avoid high concentrations of laminin and fibronectin.

Hair examination helps diagnose rare neurological diseases in children.

Neurotrophins may contribute to genetic hair thinning by inhibiting hair growth.

A person had two different benign skin tumors, a trichoadenoma and melanocytic naevi, at the same time but in different places on the face.

D-OCT shows increased blood vessel growth in response to tissue damage in Frontal Fibrosing Alopecia and is useful for diagnosis and monitoring.

Immune cells boost stem cell activity in hairy moles, causing more hair growth.

Snail1 may contribute to fibrosis in frontal fibrosing alopecia in postmenopausal women.

Researchers found a potential new type of skin growth called follicular mucinous nevus.

Nevoid basal cell carcinomas start in the skin's top layer and hair follicles.

A hair cyst can become cancerous, showing specific keratins from the hair sheath.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

Nevus psiloliparus lacks mature hair follicles but keeps other skin structures intact.

The tumor on the man's nose was a rare type called pedunculated follicular hamartoma.

Moles may stop growing because of cell cooperation, not just because of aging cells.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.